ACR Meeting Abstracts

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Abstracts tagged "Macrophage"

  • Abstract Number: 2580 • 2017 ACR/ARHP Annual Meeting

    Exploiting Inhibition of PD1 Signaling in a Murine Model of Anti-SSA/Ro Associated Congenital Heart Block

    Robert M. Clancy1, Glenn Fishman1, Colin Phoon1, Marc Halushka2, Tanisha Jackson1, Kimberly Robins1 and Jill P. Buyon1, 1NYU School of Medicine, New York, NY, 2Johns Hopkins University School of Medicine, Baltimore, MD

    Background/Purpose: The most serious manifestation of fetal exposure to maternal anti-Ro antibodies is the development of heart block. This work addresses the hypothesis that fetal…
  • Abstract Number: 2815 • 2017 ACR/ARHP Annual Meeting

    Pathological Roles By Siglec and Type I Interferons for the Development of Autoimmune Congenital Heart Block

    Robert M. Clancy1, Marc Halushka2 and Jill P. Buyon1, 1NYU School of Medicine, New York, NY, 2Johns Hopkins University School of Medicine, Baltimore, MD

    Background/Purpose: Given that diseases associated with anti-SSA/Ro such as SLE and Sjögren’s syndrome associate with an upregulation of type I interferons, recent attention has focused…
  • Abstract Number: 2926 • 2017 ACR/ARHP Annual Meeting

    Fucosyltransferase-1 Mediates Macrophage Driven Myofibroblast Differentiation and TGF-β Signaling in Systemic Sclerosis and Bleomycin-Induced Fibrosis

    W. Alexander Stinson1, Ellen Cealey1, Pei-Suen Tsou1, Ray A. Ohara1, Yuxuan Du2, Jonatan Hervoso1, Nicholas Lepore1, Sarah Arwani1, Dinesh Khanna1, David A. Fox1 and M. Asif Amin1, 1Division of Rheumatology and Clinical Autoimmune Center of Excellence, University of Michigan, Ann Arbor, MI, Ann Arbor, MI, 2Division of Rheumatology and Clinical Autoimmune Center of Excellence, University of Michigan, Ann Arbor, MI, Ann Arbor, MI, MI

    Background/Purpose: Systemic sclerosis (SSc) is a connective tissue disease characterized by dysregulated fibrosis of the skin. During fibrosis, macrophage release of transforming growth factor (TGF-β)…
  • Abstract Number: 2934 • 2017 ACR/ARHP Annual Meeting

    Comparative Analysis of the Macrophage Glycolytic Machinery in Giant Cell Arteritis (GCA) and in Coronary Artery Disease (CAD)

    Cornelia M. Weyand1, Ryu Watanabe2, Tsuyoshi Shirai3, Hui Zhang4, Gerald Berry5 and Jorg Goronzy6, 1Medicine: Immunology and Rheumatology, Stanford University, Stanford, CA, 2Medicine: Immunology/Rheumatology, Stanford University School of Medicine, Stanford, CA, 3Department of Hematology and Rheumatology, Tohoku University Graduate School of Medicine, Sendai, Japan, 4Medicine: Immunology and Rheumatology, Stanford University School of Medicine, Stanford, CA, 5Pathology, Stanford University School of Medicine, Stanford, CA, 6Medicine/Division of Immunology & Rheumatology, Stanford University School of Medicine, Stanford, CA

    Background/Purpose: Macrophages are key effector cells in the vessel wall inflammation of the atherosclerotic plaque as well as in the intramural infiltrates of giant cell…
  • Abstract Number: 284 • 2017 ACR/ARHP Annual Meeting

    Metabolic Activity Sustains Macrophage Cytokine Production in Rheumatoid Arthritis and Coronary Artery Disease

    Cornelia M. Weyand1, Markus Zeisbrich1, Lukas Brosig2, Barbara Wallis1, Niall Roche3, Janice Lin1 and Jorg Goronzy4, 1Medicine: Immunology and Rheumatology, Stanford University, Stanford, CA, 2Medicine: Immunology and Rheumatology, Stanford University, Stanfod, CA, 3The Arthritis Center, Pleasanton, CA, 4Medicine/Division of Immunology & Rheumatology, Stanford University School of Medicine, Stanford, CA

    Background/Purpose: Accelerated atherosclerosis has become increasingly recognized as a complication of chronic inflammatory disease, such as in patients with rheumatoid arthritis (RA). RA patients have…
  • Abstract Number: 285 • 2017 ACR/ARHP Annual Meeting

    Liver X Receptor-α (LXRα) Modulates Macrophage Phenotype and Disease Activity in SLE

    Shuhong Han1, Haoyang Zhuang1, Pui Lee2, Stepan Shumyak1, Jingfan Wu1, Chao Xie3, Hui Li3, Lijun Yang3 and Westley Reeves4, 1Medicine, University of Florida, Gainesville, FL, 2Harvard Medical School, Boston, MA, 3Pathology, Immunology and laboratory medicine, University of Florida, Gainesville, FL, 4Rheumatology & Clinical Immology, University of Florida, Gainesville, FL

    Background/Purpose: LXRα is an oxysterol-regulated transcription factor that plays a key role in reverse cholesterol transport by inducing the expression of ATP binding cassette A1…
  • Abstract Number: 286 • 2017 ACR/ARHP Annual Meeting

    Serum Amyloid a Aggravates Rheumatoid Arthritis By Activating NFAT5-Mediated Migration of Macrophages

    Yu-Mi Kim Sr.1, Donghyun Kim Sr.1, Seung-Ah Yoo Sr.2, Jung Hee Koh Sr.2, Jin-Sun Kong Sr.2 and Wan-Uk Kim Sr.3, 1Center for Integrative Rheumatoid Transcriptomics and Dynamics, The Catholic University of Korea, Seoul, Korea, Republic of (South), 2The Catholic University of Korea, Center for Integrative Rheumatoid Transcriptomics and Dynamics, seoul, Korea, Republic of (South), 3The Catholic University of Korea, Department of Internal Medicine, seoul, Korea, Republic of (South)

    Background/Purpose: Serum amyloid A (SAA) is an acute phase protein and its serum levels may increase up to 1000-fold over normal levels during inflammation, triggering…
  • Abstract Number: 287 • 2017 ACR/ARHP Annual Meeting

    Anti-TNF Agents Induce Alternative Macrophages

    Yannick Degboé1, Benjamin Rauwel2, Michel Baron2, Jean Frédéric Boyer2, Alain Cantagrel2, Arnaud Constantin3 and Jean-Luc Davignon2, 1Centre de Physiopathologie Toulouse Purpan, INSERM UMR 1043, Toulouse, France, 2CPTP, INSERM UMR 1043, Toulouse, France, 3Department of Rheumatology, Purpan Hospital, Toulouse III University, Toulouse, France, Toulouse, France

    Background/Purpose: Macrophages contribute to the pathogenesis of rheumatoid arthritis (RA). They can display various states of activation or « polarization », characterized by distinct functions…
  • Abstract Number: 302 • 2017 ACR/ARHP Annual Meeting

    From Monocytes to Macrophages:  the Pathogeneses of Spontaneous Inflammatory Arthritis in CD11c-Flip-KO (HUPO) Mice

    Qi Quan Huang1, Renee E. Doyle2, Philip J. Homan1, Harris Perlman3, Deborah R. WInter3 and Richard M. Pope2, 1Division of Rheumatology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, 2Medicine/Rheumatology, Northwestern University Feinberg School of Medicine, Chicago, IL, 3Department of Medicine Division of Rheumatology, Northwestern University Feinberg School of Medicine, Chicago, IL

    Background/Purpose: We have generated a CD11c-Flip-KO mouse line (HUPO) that spontaneously develops erosive arthritis with incidence 70-80% at age ≥ 20 weeks. This study aimed…
  • Abstract Number: 406 • 2017 ACR/ARHP Annual Meeting

    Mapping Changes in Monocyte and Macrophage Populations in the Synovium: An Aging Study in Arthritic KRN Ag7 Mice

    Anna B Montgomery1, Carla Cuda2, Philip J. Homan3, Harris Perlman2 and Deborah R. WInter2, 1Division of Rheumatology, Northwestern University Feinberg School of Medicine, Chicago, IL, 2Department of Medicine Division of Rheumatology, Northwestern University Feinberg School of Medicine, Chicago, IL, 3Division of Rheumatology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL

    Background/Purpose: Rheumatoid arthritis (RA) is an autoimmune disease of the joints associated with accelerated aging and increased mortality. Further, RA is linked with a number…
  • Abstract Number: 481 • 2017 ACR/ARHP Annual Meeting

    Immunocompetent Cells Expressing Citrullinated Proteins in Joint Synovium of Osteoarthritis and Rheumatoid Arthritis

    Kyoko Honne1, Masahiro Iwamoto2, Shunichiro Hanai1, Satoshi Machida3, Hitoshi Sekiya4, Reina Tsuda5, Tatsuhiko Ozawa5, Tadayoshi Karasawa6, Atsushi Muraguchi5, Masafumi Takahashi6, Hiroyuki Kishi5 and Seiji Minota7, 1Division of Rheumatology and Clinical Immunology, Jichi Medical University, Shimotsuke, Japan, 2Deivision of Rheumatology and Clinical Immunology, Jichi Medical University, Shimotsuke, Japan, 3Department of Orthopaedic Surgery, Orthopedics Clinic Medical Papas, Tochigi, Japan, 4Department of orthopedic surgery, Jichi Medical University, Shimotsuke, Japan, 5Department of Immunology, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama, Japan, 6Division of Inflammation Research Center for Molecular Medicine, Jichi Medical University, Shimotsuke, Japan, 7Division of Rheumatology and Clinical Immunology, Jichi Medical University, Tochigi, Japan

    Background/Purpose: Human monoclonal ACPA (Human-ACPA) is reported to strongly bind to synovium in RA patients [1]. The aims of our study were 1) To investigate…
  • Abstract Number: 488 • 2017 ACR/ARHP Annual Meeting

    Increased Expression of TNF-α and PAD-2 in Human Monocytes Following Treatment with Protein Modified with Malondialdehyde-Acetaldehyde (MAA) and Citrulline

    Logan M. Duryee1, Michael J. Duryee2, Dahn L Clemens1, Evan M. Ryan1, Carlos D. Hunter2, Lynell W. Klassen3, James R. O'Dell3, Daniel R. Anderson1, Ted R. Mikuls4 and Geoffrey M. Thiele1, 1University of Nebraska Medical Center, Omaha, NE, 2Internal Medicine Division of Rheumatology, University of Nebraska Medical Center, Omaha, NE, 3Department of Internal Medicine, University of Nebraska Medical Center, Omaha, NE, 4Internal Medicine, Division of Rheumatology, University of Nebraska Medical Center, Omaha, NE

    Background/Purpose:  We have previously shown that malondialdehyde-acetaldehyde (MAA) and citrullinated proteins are present together in the synovial tissues of rheumatoid arthritis (RA) patients.  Macrophage are…
  • Abstract Number: 968 • 2017 ACR/ARHP Annual Meeting

    Mononuclear Phagocytes Mediate Systemic Autoimmune Disease-Related Valvular Heart Disease Via Inflammatory Cytokine Production and Recruitment of Tissue-Reparative macrophages

    Lee Meier1, Jennifer L. Auger2, Brianna J. Engelson3, Hannah Cowan3, Elise Breed4, Mayra Gonzalez-Torres5, Joshua Boyer6 and Bryce A. Binstadt7, 1Peadiatrics, University of Minnesota, Minneapols, MN, 2Center for Immunology and Department of Pediatrics, University of Minnesota, Minneapolis, MN, 3Pediatrics, University of Minnesota, Minneapolis, MN, 4University of Minnesota Medical School, Minneapolis, MN, 5University of Puerto Rico, Ponce, Puerto Rico, 6University of California, San Diego, San Diego, CA, 7remove this, remove this, remove this, MN

    Background/Purpose:Cardiovascular comorbidity is significant in patients with systemic autoimmune diseases including rheumatoid arthritis and systemic lupus erythematosus . T cell receptor transgenic K/B.g7 mice develop…
  • Abstract Number: 2414 • 2016 ACR/ARHP Annual Meeting

    Microrna Associated with Active Systemic Juvenile Idiopathic Arthritis Regulate CD163 Expression in Polarized Macrophages through Two Distinct Mechanisms

    Thuy Do1, Rachel Tan2, Mark Bennett2, Mario Medvedovic2, Nan Shen3, Sherry Thornton1, Alexei Grom1 and Grant Schulert4, 1Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 2University of Cincinnati, Cincinnati, OH, 3Center for Autoimmune Genomics and Etiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 4Pediatric Rheumatology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH

    Background/Purpose:  CD163 is a hemoglobin scavenger receptor and innate pattern recognition receptor, and a marker of activated monocytes and macrophages. It is also expressed on…
  • Abstract Number: 2419 • 2016 ACR/ARHP Annual Meeting

    Single-Cell Analysis of CD163 mRNA and Protein Expression By Primeflow™ in Polarized Monocyte and Macrophage Populations

    Rachel Tan1, Sherry Thornton2, Alyssa Sproles2, Thuy Do3, Jonathan Schick4, Monica DeLay4 and Grant Schulert5, 1University of Cincinnati, Cincinnati, OH, 2Division of Rheumatology, Cincinnati Children's Hospital, Cincinnati, OH, 3Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 4Cincinnati Children's Hospital, Cincinnati, OH, 5Pediatric Rheumatology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH

    Background/Purpose:  CD163 is involved in the regulation and resolution of innate inflammation and the removal of free hemoglobin from the blood via internalization of the…
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All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM ET on November 14, 2024. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

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